rs63749854

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	6	Lynch syndrome, pathogenic mutation

Make rs63749854(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47478336

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63749854
dbSNP (classic)	rs63749854
ClinGen	rs63749854
ebi	rs63749854
HLI	rs63749854
Exac	rs63749854
Gnomad	rs63749854
Varsome	rs63749854
LitVar	rs63749854
Map	rs63749854
PheGenI	rs63749854
Biobank	rs63749854
1000 genomes	rs63749854
hgdp	rs63749854
ensembl	rs63749854
geneview	rs63749854
scholar	rs63749854
google	rs63749854
pharmgkb	rs63749854
gwascentral	rs63749854
openSNP	rs63749854
23andMe	rs63749854
SNPshot	rs63749854
SNPdbe	rs63749854
MSV3d	rs63749854
GWAS Ctlg	rs63749854

Max Magnitude

6

ClinVar
Risk	rs63749854(T;T)
Alt	rs63749854(T;T)
Reference	Rs63749854(G;G)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47705475G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076448.2, RCV000223378.1,